Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136677422C>A , CM000671.2:g.136677422C>A | GRCh38 |
| NC_000009.11:g.139571874C>A , CM000671.1:g.139571874C>A | GRCh37 |
| NC_000009.10:g.138691695C>A | NCBI36 |
| NG_008090.1:g.15038G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006412.4:c.316+1G>T MANE Select | NP_006403.2:n.316+1G>T |
| ENST00000371696.7:c.316+1G>T MANE Select | ENSP00000360761.2:n.316+1G>T |
| NM_001012727.1:c.316+1G>T | NP_001012745.1:n.316+1G>T |
| NM_001012727.2:c.316+1G>T | NP_001012745.1:n.316+1G>T |
| NM_006412.3:c.316+1G>T | NP_006403.2:n.316+1G>T |
| ENST00000371694.7:c.316+1G>T | ENSP00000360759.3:n.316+1G>T |
| ENST00000371696.6:c.316+1G>T | ENSP00000360761.2:n.316+1G>T |
| ENST00000470861.1:n.325G>T | |
| ENST00000538402.1:c.316+1G>T | ENSP00000438919.1:n.316+1G>T |